Hakutulokset - Christiane Penet

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  1. 1
    Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

    Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia Tekijä Alexandra Dürr, Mireille Cossée, Y. Agid, Victoria Campuzano, Claude Mignard, Christiane Penet, Jean‐Louis Mandel, Alexis Brice, Michel Kœnig

    Julkaistu 1996
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  2. 2
    Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

    Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism Tekijä Cécile Dumanchin, A. Camuzat, Dominique Campion, Patrice Verpillat, Didier Hannequin, Bruno Dubois, Pascale Saugier‐Veber, Cosette Martin, Christiane Penet, F. Charbonnier, Y. Agid, Thierry Frébourg, Alexis Brice

    Julkaistu 1998
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  3. 3
    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum Tekijä Dominique Campion, Cécile Dumanchin, Didier Hannequin, Bruno Dubois, Serge Belliard, Michèle Puel, Catherine Thomas-Antérion, Agnès Michon, Cosette Martin, Françoise Charbonnier, Grégory Raux, Agnès Camuzat, Christiane Penet, Valérie Mesnage, María Martínez, Françoise Clerget‐Darpoux, Alexis Brice, Thierry Frébourg

    Julkaistu 1999
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  4. 4
    Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

    Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Tekijä Mohamad Saad, Suzanne Lesage, Aude Saint-Pierre, Jean‐Christophe Corvol, Diana Zélénika, Jean‐Charles Lambert, Marie Vidailhet, George D. Mellick, Ebba Lohmann, F. Durif, Pierre Pollak, Philippe Damier, François Tison, Peter A. Silburn, Christophe Tzourio, Sylvie Forlani, Marie‐Anne Loriot, Maurice Giroud, Catherine Helmer, Florence Portet, Philippe Amouyel, Mark Lathrop, Alexis Elbaz, Alexandra Dürr, María Martínez, Alexis Brice, Y. Agid, Mathieu Anheim, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, Alexandra Dürr, F. Durif, Sonja Klebe, Ebba Lohmann, María Martínez, Christiane Penet, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, Marc Vérin, François Viallet, Marie Vidailhet

    Julkaistu 2010
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  5. 5
    The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

    The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Tekijä Sonja Klebe, Jean Louis Golmard, Michael A. Nalls, Mohamad Saad, Andrew B. Singleton, José Brás, John Hardy, Javier Simón‐Sánchez, Peter Heutink, Gregor Kuhlenbäumer, Rim Charfi, Christine Klein, J. Hagenah, Thomas Gasser, Isabel Wurster, Suzanne Lesage, D. Lorenz, Günther Deuschl, F. Durif, Pierre Pollak, Philippe Damier, François Tison, A. Dürr, Philippe Amouyel, Jean‐Charles Lambert, Christophe Tzourio, C. Maubaret, Fanny Charbonnier‐Beaupel, Khadija Tahiri, Marie Vidailhet, María Martínez, Alexis Brice, Jean‐Christophe Corvol, Y. Agid, Mathieu Anheim, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, A. Dürr, Franck Durif, Sonja Klebe, Ebba Lohmann, María Martínez, Christiane Penet, Pierre Pollak, Paul Krack, Olivier Rascol, François Tison, Christine Tranchant, Marc Vérin, François Viallet, Vincent Plagnol, José Brás, D. G. Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Philippe Amouyel, Sampath Arepalli, Guido P. H. Band, Roger A. Barker, C. Bellinguez, Yoav Ben‐Shlomo, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, B.R. Bloem, Zoltán Bochdanovits, Marina de Nadai Bonin Gomes, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Patrick F. Chinnery, S. A. Chong, C. E. Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, J.-F. Dartigues, P. Deloukas, David T. Dexter, Karin D. van Dijk, Allissa Dillman, Franck Durif, Sarah Edkins, Jonathan Evans

    Julkaistu 2013
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